The present invention relates to an endoscopic treatment method, and more specifically to an endoscopic treatment method for gastro esophageal reflux disease.
Conventionally, as treatment for gastro esophageal reflux disease (GERD), an oral treatment with a gastric acid secretion inhibitor and a surgical treatment such as laparoscopic Nissen fundoplication is known.
Oral treatment is not a fundamental treatment and needs to be taken for a long time, and symptoms may not improve.
Surgical treatment can be expected to solve the problem but is highly invasive. Since GERD is not a malignant disease such as a tumor, it is desirable that the invasiveness associated with the treatment be as small as possible.
A variety of endoscopic treatments are being considered as options other than oral and surgical treatments. The procedure described in U.S. Pat. No. 9,592,070 is known as one of endoscopic treatments. In this procedure, the mucous membrane in the vicinity of the gastroesophageal junction is resected to cause scarring at the resected site and cause stenosis. As a result, reflux of stomach contents is suppressed.
The present invention is an endoscopic treatment method in which a damaged area is formed in a digestive tract at least a portion in a circumferential direction of the digestive tract, the damaged area being formed by ablating mucosal layer while remaining the mucosal layer, and an incomplete stenosis is formed in the digestive tract during performance of a process of restoration of the damaged area.
An embodiment of the present invention will be described with reference to
When performing an endoscopic treatment method for gastro esophageal reflux disease according to the present embodiment (hereinafter, simply referred to as “treatment method”), the operator first inserts an endoscope through a natural opening such as mouth or nose of the subject (insertion step), and moves the distal end of the endoscope into the stomach (digestive tract). As the endoscope, a known flexible endoscope can be used.
Next, the operator operates the endoscope 100 to bend it. As shown in
By arranging the two sub-areas of the first area 11 and the second area 12 opposite to each other, the first boundary portion (first non-damaged area) 15 is located on the greater curvature side and the second boundary portion (second non-damaged area) 16 are located on the lesser curvature side, respectively. The first boundary portion 15 extends along the greater curvature. The second boundary 16 extends along the lesser curvature.
The width W1 of the first boundary portion 15 (the dimension in the circumferential direction of the gastroesophageal junction) is larger than the width W2 of the second boundary portion 16. For example, the width W1 is 10 to 20 millimeters, and the width W2 is 5 to 10 millimeters. In the following description, the first area 11 and the second area 12 may be collectively referred to as “sub-areas 11 and 12”.
The sub-areas 11 and 12 are respectively separated from the cardiac orifice Co by a predetermined distance D. The predetermined distance D is, for example, 5 to 10 millimeters. The predetermined distance D of the first area 11 and the predetermined distance D of the second area 12 may not be the same.
The width of the sub-areas 11 and 12 extending in an arcuate shape along the circumferential direction of the gastroesophageal junction is, for example, 10 to 20 mm. The width may be constant or may vary depending on the site. Furthermore, the width of the first area 11 and the width of the second area 12 may be different.
Next, the operator causes the treatment tool to protrude from the endoscope, and forms markings M around the treatment area 10 determined as shown in
The markings M need not be formed all around the treatment area, but may be formed at a plurality of spaced apart locations. In the treatment method of the present embodiment, since the first boundary portion 105 and the second boundary portion 106 play an important role, the markings M may be provided only around the first boundary portion 105 and the second boundary portion 106.
Next, the operator injects a liquid into the submucosal layer of each of the sub-areas 11 and 12 and expands each of the sub-areas 11 and 12 as shown in
When an endoscope having a plurality of treatment tool channels is used in step C, replacement work of the treatment tool can be omitted by passing the local injection needle or the like and the treatment tool used for marking through different treatment tool channels.
Next, the operator uses the treatment tool protruded from the endoscope to ablate the portions 11a and 12a (see
The expanded portions 11a and 12a have a positional relationship that makes it easy to face the endoscope due to the anatomical shape of the stomach bottom. Thereby, by advancing the treatment tool 150 while fixing the endoscope 100, the treatment tool 150 can be brought into contact with the mucous membrane of the target portions 11a and 12a as shown in
When a high-frequency knife is used as the treatment tool 150, the treatment tool 150 may be retracted little by little without moving the endoscope 100 from the state shown in
The operator ablates the entire mucous membrane in the portions 11a and 12a by repeating ablating while twisting or bending the endoscope 100 to change the position of the distal end of the treatment tool 150. Since the portions 11a and 12a are close to the stomach bottom, this step ablates the area on the stomach bottom side of the treatment area 10.
Next, the operator uses the treatment tool protruded from the endoscope to ablate the portions 11b and 12b closer to the anterior and posterior walls and the portions 11c and 12c (see
The portions 11b, 12b and 11c, 12c are difficult to face the endoscope 100 even if they are expanded due to the anatomical shape of the stomach. As a result, the treatment tool 150 protruding from the endoscope 100 approaches the mucous membrane in a state parallel or nearly parallel to the stomach wall.
Therefore, when using a high-frequency knife as the treatment tool 150, the treatment tool 150 is advanced along the mucous membrane Mc with the endoscope 100 fixed along the stomach wall as shown in
When the entire mucosal layer in the treatment area 10 is ablated, the treatment area 10 becomes a damaged area which is ablated while the mucosal layer remains. The operator removes the endoscope and ends the procedure. After ablation, the entire treatment area may be observed with an endoscope and additional ablation may be performed according to the observation result.
An example of the damaged area 10A after ablation is shown in
As described above, the treatment method of the present embodiment can be performed simply by ablating the treatment area 10 using the endoscope 100 and the treatment tool 150 inserted from the natural opening, so it is easy to perform. The treatment method of the present embodiment can be performed only by bringing the distal end of the treatment tool 150 close to the mucous membrane, so the degree of difficulty of the procedure is low.
In addition, since the tissue in the stomach is ablated and the esophagus is not ablated, discomfort or the like at the time of swallowing due to a strong constriction in the esophagus is hard to occur.
The treatment method of the present embodiment can be implemented simply by bringing the treatment tool close to the mucous membrane and ablating it, so it is easy to ablate the operator's intended range.
In the procedure for excising the mucous membrane, if the therapeutic effect of GERD is not sufficient due to the form of scarring after excision or the like, it is difficult to perform the same treatment again on the site from which the mucous membrane was excised.
On the other hand, although the treatment method of the present embodiment damages the mucous membrane, it remains without excision, and therefore, it can be applied to a portion where the mucous membrane excision is difficult due to tissue fibrosis and the like. In the endoscopic observation of incomplete stenosis after a predetermined period of time, if the formation of the folds 111, 112, or the like is not sufficient, ablation can be performed again on the mucosal layer (step D). Therefore, it is possible to flexibly respond to retreatment or additional treatment according to the follow-up result.
Various parameters such as the shape, size, and degree of damage of the treatment area related to ablation after the follow-up may be the same as or different from the first treatment.
The treatment method of the present embodiment uses high-frequency coagulation developed for hemostasis as a treatment principle, so there is almost no risk of perforation of the stomach wall or bleeding after treatment. In the treatment method of the present embodiment, strict control of the injection amount of liquid for expanding strictly controlled by ARMS, the amount of air supplied into the stomach, or the like is not required, and this point is also simple.
In the treatment area 10, in addition to the first boundary portion 105 forming the His angle, the second boundary 106 exists as an undamaged area between the sub-areas 11 and 12. As a result, excessive narrowing is less likely to occur in the treatment area than in the case where the treatment area is annular or is a single area with a long extension.
As described above, although an embodiment of the present invention was described, the technical scope of the present invention is not limited to the the above embodiment. In the range which does not deviate from the scope of the present invention, it is possible to change the combination of components, make various changes to or delete each component. Although some modifications are illustrated below, these are not all, and other modifications are possible. Two or more of these changes may be combined as appropriate.
In the treatment method of the present embodiment, the order which ablates a treatment area can be changed suitably. For example, portions 11a, 11b, and 11c may be ablated in any order. Alternatively, the first area 11 and the second area 12 may be ablated in parallel, or one of the first area 11 and the second area 12 may be ablated before the other is ablated.
Since the ablation in the treatment method of the present embodiment does not reach a muscle layer, the treatment method of the present embodiment can be performed even if expanding is not performed. That is, step C may be omitted.
The digestive tract used as the object of the treatment method of the present embodiment is not restricted to a stomach, and it is applicable also to esophagus or the like. For example, when the subject to be treated has symptoms of esophageal mucosal hypersensitivity, or the like, part or all of the treatment area may be located in the esophagus.
When the treatment area is set in the esophagus, if the treatment is performed over the entire area of a certain area with no gap in the circumferential direction, excessive stenosis may occur. The possibility of causing excessive stenosis can be reduced by methods such as providing a non-treatment area in a circumferential direction, providing a non-treatment area in a spiral shape, or providing a non-treatment area intermittently in the axial direction.
Moreover, the treatment method of the present embodiment is not only treatment of GERD which is dysfunction of esophagus, but can be applied to treatment of dysfunction of sphincter in other parts of digestive tract (for example, fecal incontinence which is dysfunction of anal sphincter, or the like).